A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205688



Internal ID22354349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66102259..66114400hg38UCSC Ensembl
chr15:66394597..66406738hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812142
hg1912142
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2959n152
Supporting Variantsnssv14445102
SamplesHG00733
Known GenesMEGF11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205688
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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